The Resource CO2 chemistry, edited by Rudi van Eldik, Michele Aresta ; Antonella Angelini [and twenty-four others] ; contributors

CO2 chemistry, edited by Rudi van Eldik, Michele Aresta ; Antonella Angelini [and twenty-four others] ; contributors

Label
CO2 chemistry
Title
CO2 chemistry
Statement of responsibility
edited by Rudi van Eldik, Michele Aresta ; Antonella Angelini [and twenty-four others] ; contributors
Contributor
Subject
Genre
Language
  • eng
  • eng
Summary
The Advances in Inorganic Chemistry series present timely and informative summaries of the current progress in a variety of subject areas within inorganic chemistry, ranging from bio-inorganic to solid state studies. This acclaimed serial features reviews written by experts in the field and serves as an indispensable reference to advanced researchers. Each volume contains an index, and each chapter is fully referenced. * Features comprehensive reviews on the latest developments * Includes contributions from leading experts in the field * Serves as an indispensable refe
Member of
Is Subseries of
Cataloging source
MiAaPQ
Dewey number
543.0877
Illustrations
illustrations
Index
index present
Language note
English
LC call number
QD181.C1
LC item number
.C6 2014
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
http://library.link/vocab/relatedWorkOrContributorDate
1940-
http://library.link/vocab/relatedWorkOrContributorName
  • Eldik, Rudi van
  • Aresta, M.
  • Angelini, Antonella
Series statement
Advances in Inorganic Chemistry,
Series volume
Volume 66
http://library.link/vocab/subjectName
  • Carbon dioxide
  • Chemistry, Inorganic
Label
CO2 chemistry, edited by Rudi van Eldik, Michele Aresta ; Antonella Angelini [and twenty-four others] ; contributors
Instantiates
Publication
Copyright
Note
Description based upon print version of record
Bibliography note
Includes bibliographical references at the end of each chapters and index
Carrier category
online resource
Carrier category code
cr
Content category
text
Content type code
txt
Contents
  • Front Cover; CO2 Chemistry; Copyright; Contents; Contributors; Preface; Chapter One: Personal Adventures in the Synthesis of Copolymers from Carbon Dioxide and Cyclic Ethers; 1. Introduction; 2. Carbon Dioxide as a Source of Chemical Carbon; 3. Copolymers from Oxiranes and Carbon Dioxide; 4. Block Copolymers of Polycarbonates and Lactides; 5. Terpolymers from Oxiranes and Carbon Dioxide; 6. Depolymerization of Polycarbonates; Acknowledgments; References; Chapter Two: Synthesis of Organic Carbonates; 1. Introduction; 2. Market and Production; 3. Linear Organic Carbonates
  • 3.1. Conventional synthesis3.2. Innovative synthesis; 3.2.1. Use of carbon dioxide as reactant; 3.2.2. Innovative synthesis based on urea utilization; 4. Synthesis of Organic Cyclic Carbonates; 4.1. Carboxylation of epoxides; 4.1.1. Use of conventional solvents; 4.1.2. Use of ionic liquids; 4.1.3. Use of sc-CO2; 4.1.4. Combined reaction media, sc-CO2, and ionic liquids; 4.2. Oxidative carboxylation of olefins; 4.2.1. Use of oxygen as oxidant; 4.2.2. Use of other oxidants; 4.3. Other synthetic routes to cyclic carbonates; 4.3.1. From halohydrins
  • 4.3.2. Reaction of cyclic ketals with carbon dioxide4.4. Synthesis of cyclic carbonates from propargyl alcohols; 4.5. Reaction between carbon dioxide and diols; 4.6. Reaction of urea and diols; 4.7. Reaction of carbon dioxide or urea with glycerol to afford glycerol carbonate; 4.8. Reactivity of cyclic alkylene carbonates; 5. Transesterification Reactions; 5.1. Synthesis of linear carbonates; 5.2. Synthesis of cyclic carbonates; 6. Summary; References; Chapter Three: Synthesis of Aromatic Carbamates from CO2: Implications for the Polyurethane Industry; 1. General Introduction
  • 2. Introduction to the PU Industry3. CO2 as a Raw Material for Isocyanates (Carbamates); 4. Possible Routes to Carbamates from CO2; 4.1. CO2 activation; 4.2. Ureas; 4.3. Substituted ureas; 4.4. Carbonates; 4.5. Electrochemical activation; 4.6. CO2+RNH2+ROH; 5. Synthesis of Aromatic Carbamates from CO2; 5.1. Background and hypothesis; 5.2. Methodology: Experiment and analysis; 5.3. Results, including by-product formation; 6. Conclusion; Acknowledgments; References; Chapter Four: Reactions of CO2 and CO2 Analogs (CXY with X, Y=O, S, NR) with Reagents Containing Si-H and Si-N Units
  • 1. Introduction2. CO2 Activation via Reactions with SiN and SiH Bonds; 2.1. CO2 insertion reactions into SiN bonds; 2.2. CO2 insertion reactions into SiH bonds; 3. Reactions of CO2 Analog Molecules with SiN Bonds and SiH Bonds; 3.1. Isoelectronic molecules: Carbon disulfide, and carbonyl sulfide; 3.2. Other heterocumulenes: Isocyanates and isothiocyanates; 4. Applications; 5. Conclusions and Outlook; References; Chapter Five: Recent Studies of Rhenium and Manganese Bipyridine Carbonyl Catalysts for the Electrochemical Reduction of CO2; 1. Introduction
  • 2. History of the fac-Re(bpy-R)(CO)3X Family of CO2 Reduction Catalysts
Dimensions
unknown
Edition
First edition.
Extent
1 online resource (417 p.)
Form of item
online
Isbn
9780127999296
Media category
computer
Media type code
c
Specific material designation
remote
System control number
  • (EBL)1584837
  • (SSID)ssj0001154607
  • (PQKBManifestationID)11663948
  • (PQKBTitleCode)TC0001154607
  • (PQKBWorkID)11176752
  • (PQKB)11758073
  • (MiAaPQ)EBC1584837
  • (EXLCZ)992550000001179118
Label
CO2 chemistry, edited by Rudi van Eldik, Michele Aresta ; Antonella Angelini [and twenty-four others] ; contributors
Publication
Copyright
Note
Description based upon print version of record
Bibliography note
Includes bibliographical references at the end of each chapters and index
Carrier category
online resource
Carrier category code
cr
Content category
text
Content type code
txt
Contents
  • Front Cover; CO2 Chemistry; Copyright; Contents; Contributors; Preface; Chapter One: Personal Adventures in the Synthesis of Copolymers from Carbon Dioxide and Cyclic Ethers; 1. Introduction; 2. Carbon Dioxide as a Source of Chemical Carbon; 3. Copolymers from Oxiranes and Carbon Dioxide; 4. Block Copolymers of Polycarbonates and Lactides; 5. Terpolymers from Oxiranes and Carbon Dioxide; 6. Depolymerization of Polycarbonates; Acknowledgments; References; Chapter Two: Synthesis of Organic Carbonates; 1. Introduction; 2. Market and Production; 3. Linear Organic Carbonates
  • 3.1. Conventional synthesis3.2. Innovative synthesis; 3.2.1. Use of carbon dioxide as reactant; 3.2.2. Innovative synthesis based on urea utilization; 4. Synthesis of Organic Cyclic Carbonates; 4.1. Carboxylation of epoxides; 4.1.1. Use of conventional solvents; 4.1.2. Use of ionic liquids; 4.1.3. Use of sc-CO2; 4.1.4. Combined reaction media, sc-CO2, and ionic liquids; 4.2. Oxidative carboxylation of olefins; 4.2.1. Use of oxygen as oxidant; 4.2.2. Use of other oxidants; 4.3. Other synthetic routes to cyclic carbonates; 4.3.1. From halohydrins
  • 4.3.2. Reaction of cyclic ketals with carbon dioxide4.4. Synthesis of cyclic carbonates from propargyl alcohols; 4.5. Reaction between carbon dioxide and diols; 4.6. Reaction of urea and diols; 4.7. Reaction of carbon dioxide or urea with glycerol to afford glycerol carbonate; 4.8. Reactivity of cyclic alkylene carbonates; 5. Transesterification Reactions; 5.1. Synthesis of linear carbonates; 5.2. Synthesis of cyclic carbonates; 6. Summary; References; Chapter Three: Synthesis of Aromatic Carbamates from CO2: Implications for the Polyurethane Industry; 1. General Introduction
  • 2. Introduction to the PU Industry3. CO2 as a Raw Material for Isocyanates (Carbamates); 4. Possible Routes to Carbamates from CO2; 4.1. CO2 activation; 4.2. Ureas; 4.3. Substituted ureas; 4.4. Carbonates; 4.5. Electrochemical activation; 4.6. CO2+RNH2+ROH; 5. Synthesis of Aromatic Carbamates from CO2; 5.1. Background and hypothesis; 5.2. Methodology: Experiment and analysis; 5.3. Results, including by-product formation; 6. Conclusion; Acknowledgments; References; Chapter Four: Reactions of CO2 and CO2 Analogs (CXY with X, Y=O, S, NR) with Reagents Containing Si-H and Si-N Units
  • 1. Introduction2. CO2 Activation via Reactions with SiN and SiH Bonds; 2.1. CO2 insertion reactions into SiN bonds; 2.2. CO2 insertion reactions into SiH bonds; 3. Reactions of CO2 Analog Molecules with SiN Bonds and SiH Bonds; 3.1. Isoelectronic molecules: Carbon disulfide, and carbonyl sulfide; 3.2. Other heterocumulenes: Isocyanates and isothiocyanates; 4. Applications; 5. Conclusions and Outlook; References; Chapter Five: Recent Studies of Rhenium and Manganese Bipyridine Carbonyl Catalysts for the Electrochemical Reduction of CO2; 1. Introduction
  • 2. History of the fac-Re(bpy-R)(CO)3X Family of CO2 Reduction Catalysts
Dimensions
unknown
Edition
First edition.
Extent
1 online resource (417 p.)
Form of item
online
Isbn
9780127999296
Media category
computer
Media type code
c
Specific material designation
remote
System control number
  • (EBL)1584837
  • (SSID)ssj0001154607
  • (PQKBManifestationID)11663948
  • (PQKBTitleCode)TC0001154607
  • (PQKBWorkID)11176752
  • (PQKB)11758073
  • (MiAaPQ)EBC1584837
  • (EXLCZ)992550000001179118

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